HARDY (John A.) < HARDY (John) < HARGUTT (Volker)

Facettes :

List of bibliographic references

Number of relevant bibliographic references: 34.
[0-20] [0 - 20][0 - 34][20-33][20-40]

Ident.	Authors (with country if any)	Title
000235 (2000)	Matt Farrer ; Alain Destee ; Estelle Becquet ; Fabienne Wavrant-De Vrieze ; Vincent Mouroux ; Florence Richard ; Luc Defebvre ; Sarah Lincoln ; John Hardy ; Philippe Amouyel ; Marie-Christine Chartier-Harlin	Linkage exclusion in French families with probable Parkinson's disease
000494 (2002)	Virgilio Gerald H. Evidente ; Katrina Gwinn-Hardy ; John Hardy ; Dena Hernandez ; Andrew Singleton	X-linked dystonia ("Lubag") presenting predominantly with parkinsonism: A more benign phenotype?
000615 (2002)	Ruey-Meei Wu ; Din-E Shan ; Chen-Ming Sun ; Ren-Shyan Liu ; Wuh-Liang Hwu ; Chun-Hwei Tai ; Jennifer Hussey ; Andrew West ; Katrina Gwinn-Hardy ; John Hardy ; Judy Chen ; Matt Farrer ; Sarah Lincoln	Clinical, 18F-dopa PET, and genetic analysis of an ethnic Chinese kindred with early-onset parkinsonism and parkin gene mutations
000687 (2002)	S. H. Subramony ; Dena Hernandez ; Amanda Adam ; Stephanie Smith-Jefferson ; Jennifer Hussey ; Katrina Gwinn-Hardy ; Timothy Lynch ; Olga Mcdaniel ; John Hardy ; Matt Farrer ; Andrew Singleton	Ethnic differences in the expression of neurodegenerative disease: Machado-Joseph disease in Africans and Caucasians
000727 (2002)	Virgilio Gerald H. Evidente ; Joel Advincula ; Raymund Esteban ; Paul Pasco ; Jhoe Anthony Alfon ; Filipinas F. Natividad ; Joven Cuanang ; Amado San Luis ; Katrina Gwinn-Hardy ; John Hardy ; Dena Hernandez ; Andrew Singleton	Phenomenology of "Lubag" or X-linked dystonia-parkinsonism
000818 (2003)	Haydeh Payami ; John Nutt ; Steven Gancher ; Thomas Bird ; Melissa Gonzales Mcneal ; William K. Seltzer ; Jennifer Hussey ; Paul Lockhart ; Katrina Gwinn-Hardy ; Amanda A. Singleton ; Andrew B. Singleton ; John Hardy ; Matthew Farrer	SCA2 may present as levodopa-responsive parkinsonism
000877 (2003)	Louis C. Tan ; Caroline M. Tanner ; RONG CHEN ; PIU CHAN ; Matthew Farrer ; John Hardy ; J. William Langston	Marked variation in clinical presentation and age of onset in a family with a heterozygous parkin mutation
000943 (2003)	John Hardy	Impact of Genetic analysis on Parkinson's disease research
000B83 (2004)	Sarah Furtado ; Haydeh Payami ; Paul J. Lockhart ; Melissa Hanson ; John G. Nutt ; Andrew A. Singleton ; Amanda Singleton ; Jamel Bower ; Ryan J. Utti ; Thomas D. Bird ; Raul De La Fuente-Fernandez ; Yoshio Tsuboi ; Mary L. Klimek ; Oksana Suchowersky ; John Hardy ; Donald B. Calne ; Zbigniew K. Wszolek ; Matthew Farrer ; Katrina Gwinn-Hardy ; A. Jon Stoessl	Profile of families with Parkinsonism-predominant spinocerebellar ataxia type 2 (SCA2)
000B88 (2004)	Joseph Wiley ; Timothy Lynch ; Sarah Lincoln ; Lisa Skipper ; Mary Hulihan ; David Gosal ; Gina Bisceglio ; Jennifer Kachergus ; John Hardy ; Matthew J. Farrer	Parkinson's disease in Ireland: Clinical presentation and genetic heterogeneity in patients with Parkin mutations
000C03 (2004)	Okan Dogu ; Janel Johnson ; Dena Hernandez ; Melissa Hanson ; John Hardy ; Hulya Apaydin ; Sibel Özekmekci ; Serhan Sevim ; Katrina Gwinn-Hardy ; Andrew Singleton	A consanguineous Turkish family with early-onset Parkinson's disease and an exon 4 parkin deletion
000C15 (2004)	Lorraine N. Clark ; Shehla Afridi ; Helen Mejia-Santana ; Juliette Harris ; Elan D. Louis ; Lucien J. Cote ; Howard Andrews ; Andrew Singleton ; Fabienne Wavrant De-Vrieze ; John Hardy ; Richard Mayeux ; Stanley Fahn ; Cheryl Waters ; Blair Ford ; Steven Frucht ; Ruth Ottman ; Karen Marder	Analysis of an early-onset Parkinson's disease cohort for DJ-1 mutations
000D86 (2005)	Aideen Mcinerney-Leo ; Donald W. Hadley ; Katrina Gwinn-Hardy ; John Hardy	Genetic testing in Parkinson's disease
000F40 (2005)	John Hardy ; Andrew J. Lees	Parkinson's disease : A broken nosology
001097 (2005)	Parastoo Momeni ; Chin-Song Lu ; Yah-Huei Wu Chou ; Hsiu-Chen Chang ; Rou-Shayn Chen ; Chiung-Chu Chen ; Jin-Tian Hsu ; Andrew Singleton ; John Hardy	Taiwanese cases of SCA2 are derived from a single founder
001103 (2005)	Jose Miguel Bras ; Rita Joao Guerreiro ; Maria Helena Ribeiro ; Cristina Januario ; Ana Morgadinho ; Catarina Resende Oliveira ; Luis Cunha ; John Hardy ; Andrew Singleton	G2019S dardarin substitution is a common cause of parkinson's disease in a portuguese cohort
001211 (2006)	Hon-Chung Fung ; Chiung-Mei Chen ; John Hardy ; Dena Hernandez ; Andrew Singleton ; Yih-Ru Wu	Lack of G2019S LRRK2 mutation in a cohort of taiwanese with sporadic parkinson's disease
001248 (2006)	Liana Fidani ; Kallirhoe Kalinderi ; Sevasti Bostantjopoulou ; Jordi Clarimon ; Antonis Goulas ; Zoe Katsarou ; John Hardy ; Alexandros Kotsis	Association of the Tau haplotype with Parkinson's disease in the greek population
001948 (2008)	Sarah Teixeira Camargos ; Francisco Cardoso ; Parastoo Momeni ; Juliana Gurgel Gianetti ; Andrew Lees ; John Hardy ; Andrew Singleton	Novel GCH1 Mutation in a Brazilian Family with Dopa-Responsive Dystonia
001B13 (2008)	Rita Joao Guerreiro ; Isabel Santana ; Jose Miguel Bras ; Tamas Revesz ; Olinda Rebelo ; Maria Helena Ribeiro ; Beatriz Santiago ; Catarina Resende Oliveira ; Andrew Singleton ; John Hardy	Novel Progranulin Mutation : Screening for PGRN Mutations in a Portuguese Series of FTD/CBS Cases
001D76 (2009)	Susanne A. Schneider ; Kailash P. Bhatia ; John Hardy	Complicated Recessive Dystonia Parkinsonism Syndromes

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